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Arctic rivers are sensitive to climate and environmental change, but the biogeochemical response remains poorly understood. Monthly size‐fractionated dissolved organic matter (DOM) samples from the lower Yukon River were characterized using UV–visible, fluorescence, and Fourier transform‐infrared (FT‐IR) spectroscopy techniques. The EEM‐PARAFAC analysis revealed three major fluorescent DOM components, including two humic‐like components (C480 and C400) and one protein‐like component (C310), with their relative importance following the order of C480 ≥ C400 > C310 in the high‐molecular‐weight DOM (1 kDa–0.4 μm) and C400 > C480 > C310 in the low‐molecular‐weight DOM pool (< 1 kDa). Transformation in DOM and change in sources were manifested in major fluorescent components and optical properties, including biological index (BIX), humification index (HIX), spectral slope (S275–295) and specific UV absorbance at 254 nm (SUVA254). These changes occurred within different DOM size‐fractions and among ice‐covered, spring freshet, and open seasons. Joint analysis of EEM and FT‐IR spectra using a data fusion technique showed that humic‐like DOM is mostly associated with C─H, C═C, and C─O bonds, while protein‐like DOM is correlated more with C─N and N─H related structures. DOM aromaticity and the ratios of HIX to BIX and protein‐like to humic‐like components may be used as a compelling proxy to measure change in source waters and to infer permafrost dynamics. Our results provide insight into the seasonal variation in DOM composition for different size‐fractions in the lower Yukon River, and a baseline dataset against which future changes can be understood in the context of arctic basin biogeochemical cycling. [ABSTRACT FROM AUTHOR]

Abstract: Dissolved organic matter (DOM) plays a significant role in freshwater and marine aquatic ecosystems including its effects on nutrients and carbon cycling and trace metal and contaminant availability. The colored fraction of DOM, CDOM, directly affects the quantity and spectral quality of available light, thereby impacting both primary production and UV exposure in aquatic ecosystems. Measuring the DOM absorption coefficient in situ is difficult because it requires prefiltration of the sample. From measurements made in inland, riverine, estuarine and coastal environments, we show that using the WETStar fluorometer (WET Labs), good estimates of dissolved absorption can be obtained from DOM fluorescence (DOM-FL) measured in situ on unfiltered samples. DOM-FL measured with the in situ fluorometer compare very well to values obtained on filtered samples using more sophisticated laboratory spectrofluorometers. Acquisition of high frequency, long-term data series or high-resolution profiles is feasible and artifacts resulting from filtration or sample storage can be avoided when measurements are made using the WETStar DOM fluorometer. The utility of high-resolution DOM-FL profiles for biogeochemical studies is illustrated by in situ data obtained in the East Siberian Sea. [Copyright &y& Elsevier]